Canonical Allele Identifier: PA2826320567
Gene: TCF4 HGNC NCBI

Linked Data

ClinVar Variation Id: 2240625
ClinVar RCV Id: RCV002719286

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001230159.1:p.Ser303Gly
CA402701102
NM_001243230.2:c.907A>G